NDC Code | 43386-670-01 |
Package Description | 100 TABLET in 1 BOTTLE (43386-670-01) |
Product NDC | 43386-670 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pentazocine Hydrochloride And Acetaminophen |
Non-Proprietary Name | Pentazocine Hydrochloride And Acetaminophen |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20110511 |
Marketing Category Name | ANDA |
Application Number | ANDA076202 |
Manufacturer | GAVIS Pharmaceuticals, LLC |
Substance Name | PENTAZOCINE HYDROCHLORIDE; ACETAMINOPHEN |
Strength | 25; 650 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA] |
DEA Schedule | CIV |